Article R313-17-2
If the assigned receivable includes a portion representing a fraction of the cost of the investments, as defined pursuant to Article L. 313-29-1 of the French Monetary and Financial Code, the notifica…
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Showing 801–810 of 3970 articles for “Art. CE 29 January 1982 n° 18058”
If the assigned receivable includes a portion representing a fraction of the cost of the investments, as defined pursuant to Article L. 313-29-1 of the French Monetary and Financial Code, the notifica…
A Conseil d'Etat decree defines the terms and conditions for the application of 27°, 28° and 29° of article L. 2321-2; in particular, it defines the fixed assets that are subject to the depreciation o…
All in vitro diagnostic medical devices imported, placed on the market or put into service must bear the CE mark. However, CE marking is not required for devices undergoing a performance evaluation or…
…LE D. 110-1LIST OF BILATERAL AGREEMENTS AND CONVENTIONS DEFINING THE CONDITIONS OF ENTRY AND RESIDENCE ON FRENCH TERRITORY FOR NATIONALS OF THE STATES WITH WHICH THEY HAVE BEEN CONCLUDEDThe bilateral…
The affixing of marks or inscriptions on a medical device, on its packaging or on the instructions for use which are likely to mislead as to the meaning or form of the CE marking is prohibited. Any ot…
As part of its mission to receive asylum seekers as defined in Article L. 121-1 of the Labour Code, the French Office for Immigration and Integration coordinates the management of accommodation in the…
The provisions of this section will be repealed five years after 9 January 1993, the date of publication of the loi n° 93-23 du 8 janvier 1993 modifiant le titre VI du livre III du code des communes e…
Any medical device placed on the market or put into service in France must bear the CE mark certifying that it meets the conditions set out in article R. 5211-17. However, CE marking is not required f…
The State defines and implements national tourism policy. It determines and implements the procedures for approving and classifying tourist facilities, organisations and activities in accordance with…
The CE mark is affixed under the responsibility of the manufacturer or his authorised representative. Its form and dimensions are laid down by order of the Minister for Health. The CE marking must be…
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